BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

262 related articles for article (PubMed ID: 21416596)

  • 1. Discordant phenotypes in a mother and daughter with mosaic supernumerary ring chromosome 19 explained by a de novo 7q36.2 deletion and 7p22.1 duplication.
    Argiropoulos B; Carter M; Brierley K; Hare H; Bouchard A; Al-Hertani W; Ryan SR; Reid J; Basik M; McGowan-Jordan J; Graham GE
    Am J Med Genet A; 2011 Apr; 155A(4):885-91. PubMed ID: 21416596
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cytogenomic and phenotypic analysis in low-level monosomy 7 mosaicism with non-supernumerary ring chromosome 7.
    Salas-Labadía C; Cervantes-Barragán DE; Cruz-Alcívar R; Daber RD; Conlin LK; Leonard LD; Spinner NB; Durán-McKinster C; Dávila-Ortíz de Montellano DJ; Del Castillo-Ruiz V; Pérez-Vera P
    Am J Med Genet A; 2014 Jul; 164A(7):1765-9. PubMed ID: 24677512
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recombinant chromosome 7 in a mosaic 45,X/47,XXX patient.
    Tirado CA; Gotway G; Torgbe E; Iyer S; Dallaire S; Appleberry T; Suterwala M; Garcia R; Valdez F; Patel S; Koduru P
    Am J Med Genet A; 2012 Jan; 158A(1):206-14. PubMed ID: 22106088
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mild phenotype in a patient with mosaic del(8p)/inv dup del(8p).
    Hand M; Gray C; Glew G; Tsuchiya KD
    Am J Med Genet A; 2010 Nov; 152A(11):2827-31. PubMed ID: 20830805
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Siblings with opposite chromosome constitutions, dup(2q)/del(7q) and del(2q)/dup(7q).
    Shim SH; Shim JS; Min K; Lee HS; Park JE; Park SH; Hwang E; Kim M
    Gene; 2014 Jan; 534(1):100-6. PubMed ID: 24095776
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient.
    Lukusa T; Van Buggenhout G; Devriendt K; Fryns JP
    Genet Couns; 2002; 13(1):1-10. PubMed ID: 12017231
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Lee MS; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):705-711. PubMed ID: 27751420
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disability.
    Chen CP; Lin SP; Chern SR; Tsai FJ; Lee MS; Chen YJ; Wang W
    Genet Couns; 2011; 22(4):425-30. PubMed ID: 22303804
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of a de novo Supernumerary Neocentric Ring Chromosome Derived from Chromosome 7.
    Louvrier C; Egea G; Labalme A; Des Portes V; Gazzo S; Callet-Bauchu E; Till M; Sanlaville D; Edery P; Schluth-Bolard C
    Cytogenet Genome Res; 2015; 147(2-3):111-7. PubMed ID: 26669311
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic spectrum of interstitial 7p duplication in mosaic and non-mosaic forms.
    Cox H; Stewart H; Hall L; Donnai D
    Am J Med Genet; 2002 May; 109(4):306-10. PubMed ID: 11992485
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structural abnormalities of chromosome 8 and fetoplacental discrepancy: A second case report and review of fetal phenotype of 8p inverted duplication deletion syndrome.
    Huynh MT; Riteau AS; Moradkhani K; Pichon O; Richard S; Joubert M; Bézieau S
    Eur J Med Genet; 2021 Jan; 64(1):104118. PubMed ID: 33248287
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
    Eyüpoğlu FC; Sünnetçi D; Cine N; Savli H; Okten A; Açikgöz EG; Sönmez FM
    Genet Couns; 2014; 25(3):305-13. PubMed ID: 25365853
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
    Chen CP; Lin SP; Lin YH; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A report of pure 7p duplication syndrome and review of the literature.
    Papadopoulou E; Sifakis S; Sarri C; Gyftodimou J; Liehr T; Mrasek K; Kalmanti M; Petersen MB
    Am J Med Genet A; 2006 Dec; 140(24):2802-6. PubMed ID: 17103460
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings.
    Shojaei A; Behjati F; Derakhshandeh-Peykar P; Razzaghy-Azar M; Otukesh H; Kariminejad R; Dowlati MA; Rashidi-Nezhad A; Tavakkoly-Bazzaz J
    Gene; 2013 Mar; 517(1):137-45. PubMed ID: 23201896
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
    Chen CP; Ko TM; Su YN; Wang LK; Chern SR; Wu PS; Chen YN; Chen SW; Ko K; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Case report of rec(7)dup(7q)inv(7)(p22q22) and a review of the recombinants resulting from parental pericentric inversions on any chromosomes.
    Ishii F; Fujita H; Nagai A; Ogihara T; Kim HS; Okamoto R; Mino M
    Am J Med Genet; 1997 Dec; 73(3):290-5. PubMed ID: 9415687
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pallister-Killian syndrome caused by mosaicism for a supernumerary ring chromosome 12p.
    Yeung A; Francis D; Giouzeppos O; Amor DJ
    Am J Med Genet A; 2009 Mar; 149A(3):505-9. PubMed ID: 19215037
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis.
    Bartsch O; Vlcková Z; Erdogan F; Ullmann R; Novotná D; Spiegel M; Beyer V; Haaf T; Zechner U; Seemanová E
    Cytogenet Genome Res; 2007; 119(1-2):158-64. PubMed ID: 18160797
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.